De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy
- Lieve Claes
- , Berten Ceulemans
- , Dominique Audenaert
- , Katrien Smets
- , Ann Löfgren
- , Jurgen Del-Favero
- , Sirpa Ala-Mello
- , Lina Basel-Vanagaite
- , Barbara Plecko
- , Salmo Raskin
- , Paul Thiry
- , Nicole I Wolf
- , Christine Van Broeckhoven
- , Peter De Jonghe
Onderzoeksoutput: Article › peer review
177
Citaten
(Scopus)